Hexachlorocyclopentadiene adducts of unsaturated amides

ABSTRACT

THIS INVENTION RELATIVES TO CERTAIN NEW NITROGEN-CONTAINING COMPOUNDS, MORE PARTICULARLY TO N-SUBSTITUTED AND N,N-DISUBSTITUTED AMIDES, THE ACYL MOIETIES OF WHICH ARE THE ACYL MOIETIES OF TH HEXACHLOROCYCLOPENTADIENE ADDUCTS OF EITHER 9-OCTADECNOIC OR 10-UNDECENOIC ACIDS. THE COMPOUNDS WHICH ARE THE SUBJECT OF THIS INVENTION ARE CHARACTERIZED BY THE FACT THAT AS GROWTH INHIBITORS THEY ARE EFFECTIVE AGAINST A VARIETY OF BACTERIA, YEASTS, AND MOLDS, SOME OF WHICH ARE PATHOGENIC. THEY ARE ALSO USEFUL AS PLASTICIZERS.

United States Patent 3,794,640 HEXACHLOROCYCLOPENTADIENE ADDUCTS 0F UNSATURATED AMIDES Robert R. Mod, Frank C. Magne, and Evald L. Skau,

New Orleans, La., assignors to the United States of America as represented by the Secretary of Agriculture No Drawing. Original application Nov. 21, 1969, Ser. No. 878,922, now Patent No. 3,663,582. Divided and this application Dec. 16, 1971, Ser. No. 208,946

Int. Cl. C07d 87/34 US. Cl. 260247.7 H 1 Claim ABSTRACT OF THE DISCLOSURE This invention relates to certain new nitrogen-containing compounds, more particularly to N-substituted and N,N-disubstituted amides, the acyl moieties of which are the acyl moieties of the hexachlorocyclopentadiene adducts of either 9-octadecenoic or IO-undecenoic acids.

The compounds which are the subject of this invention are characterized by the fact that as growth inhibitors they are effective against a variety of bacteria, yeasts, and molds, some of which are pathogenic. They are also useful as plasticizers.

This is a division of application Ser. No. 878,922, filed Nov. 21, 1969, now US. Pat. No. 3,663,582.

A non-exclusive, irrevocable, royalty-free license in the invention herein described, throughout the world for all purposes of the United States Government, with the power to grant sublicenses for such purposes, is hereby granted to the Government of the United States of America.

The compounds which are the subject of this inventioninclude N-acyl derivatives of the following primary and secondary amines and cyclic irnines: dimethylamine, diethylamine, dibutylamine, N -methylpropylamine, N- methyl-butylamine, allylamine, N-methyl-allylamine, N,N- bis(2-ethoxyethyl)amine, N-ethyl-2-ethoxyethylamine, N- ethyl 3 ethoxypropylamine, pyrrolidine, piperidine, 2- methylpiperidine, morpholine, azabicyclo [3 .2.2] nonane, piperazine, N-methylpiperazine, and benzylamine, the acyl group being that of the hexachlorocyclopentadiene adduct of either 9-octadecenoic or lO-undecenoic acid.

The compounds which are the subject of this invention are:

N,N dibutyl 8 (1,4,5,6,7,7 hexachloro 3 octylbicyclo[2.2.1]-5-heptene-2-yl)octanamide CH (CHz)7CHCH(CI-I2)7C ON(CH:1)2

C ClC(Cl)z-C Cl N,N dimethyl '8 (1,4,5,6,7,7 hexachloro 3 octylbicyclo[2.2.1]-5-heptene-2-yl)octanamide 0113mm).-0H-0H- 0H.)700N(02m).

CC1=C Cl N methyl N butyl 8 (1,4,5,6,7,7 hexachloro- 3-octabicyclo[2.2.1]-5-heptene-2-yl)octanamide CH3 CH (CH2)1CHOH-(CH CON C ClC(C12)-CO1 N methyl N allyl 8 (1,4,5,6,7,7 hexachloro 3- octylbicyclo [2.2.1 ]-5-heptene-2-yl) octanamide 0H.(0H2)7-0E-0H(0H,)700N(0H20H2002H5).

CClO(Cl2)CC-l CCl=COI N,N bis ('2 ethoxyethyl) 8 (1,4,5,6,7,7 hexachloro-3-0cty1bicyclo [2.2.1 -5-heptene-2-yl) octanamide CH (CH2)1-CHCH(CH;) C0N N ethyl 3 ethoxypropyl 8 (1,4,5,6,7,7 hexachloro-3-octylbicyclo[2.2. 1 -5 -heptene-2-y1)octanamide CHJ (CHZ)7 CH CH (C I)T ON o01 o c1.)o 01 N- [8 1,4,5,6,7,7-hexachloro 3 octylbicyclo [2.2.11-5- heptene-2-yl) octanoyl] pyrrolidine CH: C HzCHz 0 C 2H5 CHr-CH1 N-[8(l,4,5,6,7,7-hexachloro 3 octylbicyclo[2.2.l]-5'- heptene-Z-yl) octanoyl] piperidine N-[8(1,4,5,6,7,7-hexachloro 3 octylbicycl0[2.2.1]-5- heptene-2-y1) octanoyl] -2-methylpiperidine N-[8(1,4,5,6,7,7-hexachloro 3 octylbicyclo[2.2.1]-5- heptene-Z-yDoctanoyl]morpholine N-[8 1,4,5,6,7,7-hexachloro 3 octylbicyclo[2.2.1]-5- heptene-Z-yl) octanoyl] -3-azabicyclo [3 .2.2] nonane 3 N-benzyl-8-(1,4,5,-6,7,7 hexachloro 3 octylbicyclo- [2.2.1 --heptene-2-yl) octanamide N-methyl N propyl-9-(1,4,5,6,7,7-hexachlorobicyclo- [2.2.1]-5-heptene-2-yl)nonanamide N- [9-( 1,4,5 ,6,7 ,7 hexachlorobicyclo[2.2.11-5-heptene- 2-yl)nonanoyl] piperidine N,N'-bis[9 (1,4,5,6,7,7 hexach1orobicyclo[2.2.1]-5- heptene-2yl) nonanoyl] piperazine The new nitrogen-containing compounds which are the subject of this invention were prepared by conventional methods.

The bioactivity of these various new nitrogen-containing compounds has been established by us in vitro but, as will be obvious to those skilled in the arts pertaining to the growth inhibition of bacteria, yeast, and molds, the compounds, besides being used as such, can for utilitarian purposes be formulated using a liquid, viscous, or solid diluent. 1

The diluent or extender must be inert with respect to the compound involved and since this is the only significant requirement, a wide variety of these agents is operable, among which are petroleum jellies, various alcohols, polyols, vegetable oils, and the like.

The compounds of this invention were screened for their antimicrobial activity against two bacteria-Bacillus sp., and Pseudomonas sp.and a number of pathogenic yeasts or molds-Aspergillus flavus, Candida albicans, Microsporum gypireum, Trichophyton rubrum, and T richophyton violaceum.

Difco Bacto Dehydrated Nutrient Agar at pH 6.8, Difco Bacto Dehydrated Yeast Morphological Agar at pH 4.5, and Difco Dehydrated Mycological Agar at pH 7.0 were used to test the inhibition of the bacteria, yeast, and mold cultures, respectively. The micro-organisms used were obtained from stock cultures. Seeded agar plates were used to measure the antibacterial activity against bacteria. Hardened agar plates inoculated either by streaking or pouring the culture onto the plates were employed in the activity estimations against molds. Standard size (6.5 mm.) paper discs wetted with the test compound were placed on the surface of the agar plates inoculated with the test organisms. When streaked plates were used the test compounds were added onto the specified areas.

To eliminate any error which could result from an insufiicient number of tests, a minimum of three experiments employing duplicate plates was used for measuring the antimicrobial activity of each compound.

All test plates were incubated at the optimum growing temperature for each organism. Zones of inhibition were compared with those of the controls after periodic readings after 3, 5, and 7 days. The 7-day readings compiled in Table I show that the compounds were effective as growth inhibitors against specific organisms.

TABLE I Antimicrobial acticity B Micro-organisms b A B C D E F G o o o o oo oo oo 0 o oo o oo 0 B +=Zone of inhibition extends up to 0.5 cm. from disc; oo =organism failed to grow on disc; o=slight growth of organism on disc; =no inhibition detectable. I

b A=Aspergillus flaws; B= Candida albicans; C= Trzchophyton rubrum; D=Trichophyt0n violaceum; E=Micr0sp0rum gypseu'm; F=Baczllus sp.; G=Pseud0monas 8p.

Specific examples showing the preparation of each of the new compounds being claimed are set forth below along with appropriate data in Table I which establish the growth inhibiting properties of the claimed compounds.

EXAMPLE 1 The hexachlorocyclopentadiene adduct of oleoyl chloride was prepared by reacting, under a nitrogen blanket, grams of oleoyl chloride with 145.2 grams of hexachlorocyclopentadiene in a flask equipped with a condenser for 28 hours at C. Since neither hexachlorocyclopentadiene nor the adduct absorbs bromine, iodine values were used to determine the percentage of the oleoyl chloride converted. The reaction mixture showed a 75% conversion to the adduct. The excess hexachlorocyclopentadiene was removed by stripping at reduced pressure. Aliquots of the product, 8-(l,4,5,6,7,7-hexachloro-3-octylbicyclo [2.2. l -5-heptene-2-yl octanoyl chloride, were used to prepare the corresponding N-substituted amides described in Examples 2 to 16.

EXAMPLE 2 The N,N-dibutyl amide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by dissolving 14.6 grams of dibutylamine and 11.4 grams of triethylamine in benzene and adding dropwise with stirring 57 grams of the oleyl chloride adduct prepared by the procedure of Example 1. After stirring for an additional hour, the reaction mixture was filtered, washed successively with dilute hydrochloric acid and water, dried over anhydrous sodium sulfate, percolated through a column of activated alumina to remove residual free acid, and stripped. N,N- dibutyloleamide was removed by two urea clathrations. The product obtained by stripping the filtrate was dissolved in commercial hexane and residual urea was removed by washing with hydrochloric acid and water. The solution was dried over anhydrous sodium sulfate, filtered, and stripped. The product, N,N-dibutyl-8-(1,4,5,6,7,7- hexachloro-3-octylbicyclo[2.2.l1 5 heptene-2-yl)octanamide, gave the following analysis: percent C, 55.56 (theory 55.86); percent H, 7.62 (theory 7.71); percent N, 1.95 (theory 2.10); percent Cl, 40.84 (theory 40.59).

This compound was tested as a plasticizer for vinyl chloride-vinyl acetate (9-525) copolymer resin in the following formulation:

This formulation was milled, molded, and tested. The resulting molded plasticized resin showed no evidence of exudation or migration to the surface during shelf storage of 30 days and had the following properties: tensile strength, 3380 (3130) p.s.i.; 100% modulus, 3140 (1640) p.s.i.; elongation 260 (360) percent; brittle point, +3 (-31) C.; volatility loss 0.03 (1.5) percent, soapy water extractability 0.00 (3.0) percent. The corresponding properties using the control plasticizer, di-2ethylhexyl phthalate (DOP), in the same formulation are given in parenthesis. The compound is therefore a good compatible primary plasticizer giving a plasticized stock showing extremely low volatility loss and soapy water extractability. The plasticized resin was also less flammable than DOP.

EXAMPLE 3 The N,N-dimethylamide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 1.1 grams of anhydrous dimethylamine, 2.4 grams of methylamine, and 12 grams of the oleoylchloride adduct prepared by the procedure of Example 1. The product, N,N-dimethyl-8-(1,4,5,6,7,7-hexachloro 3 octylbicyclo[2.2.l] 5 heptene 2 yl)octanamide, gave the following analysis: percent C, 51.50 (theory 51.56); percent H, 6.73 (theory 6.75); percent N, 2.17 (theory 2.40); percent Cl, 36.48 (theory 36.53).

EXAMPLE 4 The N,N-diethyl amide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 2.7 grams of diethylamine, 3.7 grams of triethylamine and 17 grams of the oleo'yl chloride adduct prepared by the procedure of Example 1. The product, N,N-diethyl-8-(1,4,5, 6,7,7-hexachloro-3-octylbicyclo[2.2.1]-5-heptene-2-yl)octanamide, gave the following analysis: percent C, 55.09 (theory 53.12); percent H, 7.79 (theory 7.10); percent N, 2.50 (theory 2.20); percent Cl, 34.58 (theory 34.86).

EXAMPLE 5 The N-methyl-N-butyl amide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2' using 2.5 grams of N-methylbutylamine, 2.9 grams of triethylamine and 15 grams of the I oleoyl chloride adduct prepared by the procedure of Example l. The product, N-methyl-N-butyl-8-(l,4,5,6,7,7- hexachloro-3-octylbicyclo[2.2.1] 5 heptene-Z-yDoctanamide, gave the following analysis: percent C, 55.77 (theory 53.86); percent H, 7.61 (theory 7 .2 6); percent N, 2.26 (theory 2.24); percent CI, 32.07 (theory 34.07).

EXAMPLE 6 The N-meth'yl-N-allyl amide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 3.4 grams of N-methylallylamine, 4.9 grams of triethylamine and 25 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N-methyl-N-a1lyl8-(1,4,5,6,7,7- hexach1oro-3-octylbicyclo[2.2.1] 5 heptene-2-yl)octanamide, gave the following analysis: percent C, 53.90 theory 53.30); percent H, 7.22 (theory 6.79); percent N, 2.42 (theory 2.30); percent Cl, 32.84 (theory 34.97).

EXAMPLE 7 6 EXAMPLE 8 The n-ethyl-N-3-ethoxypropyl amide of the hexachloroc'yclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 3.8 grams of N-ethyl-N-3- ethoxypropylamine, 2.9 grams of triethylamine and 15 grams of the oleoyl chloride adduct prepared by the procedure of Example '1. The product, N-ethyl-N-3-ethoxypropyl-8-(1,4,5,6,7,7-hexachloro 3 octylbicyclo[2.2.l]- 5-heptene-2-yl)octanamide, gave the following analysis: percent C, 55.60 (theory 53.90); percent H, 7.70 (theory 7.39); percent N, 2.15 (theory 2.10); percent Cl, 29.63 (theory 31.83).

EXAMPLE 9 N-[-8-(1,4,5,6,7,7-hexachloro 3 octylbicyclo[2.2.1]- 5-heptene-2ryl)octanoylJpyrrolidine was prepared by the method of Example 2 using 2.1 grams of pyrrolidine, 2.9 grams of triethylamine and 15 grams of the oleoyl chlo ride adduct prepared by the procedure of Example 1. The product, N-[8-(l,4,5,6,7,7-hexachloro 3 octylbicyclo- [2.2.1]-5-heptene-2-yl)octandyl]pyrrolidine gave the following analysis: percent C, 53.34 (theory 53.30); percent H, 6.78 (theory 6.79); percent N, 2.21 (theory 2.30) percent CI, 35.13 (theory 34.97).

EXAMPLE 10 The piperidide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 2.8 grams of piperidine, 3.3 grams of triethylamine, and 15 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N [8 (1,4,5,6,7,7 hexachloro-3-octylbicyc1o[2.2.1]-5- heptene-2-yl)octanoyl]piperidine, gave the following analysis: percent C, 56.46 (theory 54.03); percent H, 7.90 (theory 6.96); percent N, 2.24 (theory 2.25); percent Cl, 29.92 (theory 34.08).

EXAMPLE 11 The Z-methylpiperidide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 3.2 grams of Z-methylpiperidine, 3.3 grams of triethylamine, and 15 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N a [8 (1,4,5,6,7,7 hexachloro-3-octylbicyclo [2.2.1] 5 heptene 2-yl)octanoyl]-2-m'ethylpiperidine, gave the following analysis: percent C, 57.28 (theory 54.73); percent H, 7.77 (theory 7.13); percent N, 2.49 (theory 2.20); percent Cl, 28.95 (theory 28.95).

EXAMPLE 12 The morpholide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 by using 2.2 grams of morpholine, 2.3 grams of triethylamine, and 11 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N [8 (1,4,5,6,7,7 hexachloro-3-octylbicyclo [2.2.1] 5 heptene-2yl)octanoyl]morpholine, gave the following analysis: percent C, 52.67 (theory 51.93); percent H, 6.80 (theory 6.62); percent N, 2.40 (theory 2.24); percent Cl, 32.83 (theory 34.08).

EXAMPLE 13 N [8 (1,4,5,6,7,7 hexachloro-3-octylbicyclo[2.2.1]- S-heptene-Z-yl)octanoylJ-3-azabicyclo[3.2.2]nonane was prepared by the procedure of Example 2 using 4 grams of 3-azabicycl'o[3.2.2] nonane, 3.3 grams of triethylamine, and 15 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N-[8-(1,4, 5,6,7,7 hexachloro ,3 octy1bicyclo[2.2.1]-5-heptene-2- yl) oetanoyl]-3-azabicyclo[3.2.2]nonane, gave the following analysis: percent C, 58.63 (theory 56.21); percent H, 7.70 (theory 7.15); percent N, 2.28 (theory 2.11); percent Cl, 27.94 (theory 32.12).

7 EXAMPLE 14 The N-allyl amide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 1.7 grams of allylamine, 2.9 grams of triethylamine, and 15 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N-allyl-8-(1,4,5,6,7,7 hexachloro-3-octylbicycl0[2.2.-]5- heptene-2-yl)octanamide, gave the following analysis: percent C, 53.38 (theory 52.54); percent H, 6.72 (theory 6.61); percent N, 2.31 (theory 2.35); percent Cl, 34.71 (theory 35.80).

EXAMPLE 15 The N-benzyl amide of the hexachlorocyclopentadiene adduct of oleic acid was prepared by the procedure of Example 2 using 3.1 grams of benzylamine, 2.9 grams of triethylamine, and 15 grams of the oleoyl chloride adduct prepared by the procedure of Example 1. The product, N benzyl 8 (1,4,5,6,7,7 hexachloro 3 octylbicyclo [2.2.1]-5-heptene-2-yl)octamide, gave the following analysis: percent C, 55.88 (theory 55.91); percent H, 6.56 (theory 6.41); percent N, 2.11 (theory 2.17); percent Cl, 33.16 (theory 33.02).

EXAMPLE 16 N [8 (1,4,5,6,7,7 hexachloro-3-octylbicyclo[2.2.1]- 5-heptene-2-yl)octanoyl]N'-rnethylpiperazine was prepared by adding dropwise with stirring 25.6 grams of the oleoyl chloride adduct of Example 1 to a benzene solution of 5 grams of N-methylpiperazine and 5.1 grams of triethylamine. After stirring for an additional hour the reaction mixture was filtered. The filtrate was dried over sodium sulfate, percolated through activated alumina to remove residual acid chloride adduct, and stripped. 25 grams of the product was added to a hot solution of methanol containing 100 grams of urea. The solution was allowed to cool to room temperature and stored at 0 C. overnight. The urea-complexed crystals were filtered and pressed dry after which an additional 100 grams of urea were dissolved in the filtrate. The crystallization and filtration were repeated. The product obtained by stripping the methanol from the filtrate was dissolved in chloroform, filtered to remove residual urea, and stripped. The product, N [8 (1,4,5,6,7,7 hexachloro-3-octylbicyclo[2.2.1]-5- heptene-2-yl)octanoyl] N-methylpiperazine, gave the following analysis: percent C, 53.99 (theory 52.76); percent H, 7.15 (theory 6.96); percent N, 5.34 (theory 4.40); percent Cl, 29.95 (theory 33.38).

EXAMPLE 17 The N-methyl-N-propyl amide of the hexachlorocyclopentadiene adduct of IO-undecenamide was prepared by reacting under a nitrogen blanket 7 grams of N-methyl-N- propyl-lO-undecenamide with 8 grams of hexachlorocyclopentadiene in a flask equipped with a condenser for 10 hours at 135 C. The reaction mixture was dissolved in methyl alcohol and filtered. Unreacted hexachlorocyclopentadiene was removed by stripping under reduced pressure. Unreacted amide was removed by two urea clathrations. The product, N-methyl-N-propyl-9-(1,4,5, 6,7,7 hexachlorobicyclo[2.2.1] 5 heptene 2 yl)nonamide, gave the following analysis: percent C, 48.80 (theory 46.90); percent H, 6.31 (theory 5.71); percent N, 2.92 (theory 2.74); percent CI, 40.92 (theory 41.54).

EXAMPLE 18 The hexachlorocyclopentadiene adduct of IO-undecenoyl chloride was prepared from IO-undecenoyl chloride by the procedure of Example 1. Aliquots of the product, 9 (1,4,5,6,7,7-hexachlorobicyclo[2.2.11-5-heptene-2-yl)nonanoyl chloride, were used to prepare the N-substituted amides of Examples 19 and 20.

EXAMPLE 19 The piperidide of the hexachlorocyclopentadiene adduct of IO-undecenoic acid was prepared by the procedure of Example 2 using 3. 6 grams of piperidine, 4.3 grams of triethylamine, and 20 grams of the IO-undecenoyl chloride adduct prepared in Example 18. The product N-[9-(1,4,5, 6,7,7 hexachlorobicyclo[2.2.1] 5 heptene 2 yl)nonanoyl]piperidine, gave the following analysis: percent C, 48.01 (theory 48.12); percent H, 5.63 (theory 5.58); percent N, 2.50 (theory 2.67); percent Cl, 40.84 (theory 40.59).

EXAMPLE 20 N,N bis [9 (1,4,5,6,7,7 hexachlorobicyclo[2.2.1]-5- heptene-2-yl)nonanoyl]piperazine was prepared by the procedure of Example 2 using 1.8 grams anhydrous piperazine, 4.3 grams triethylamine, and 20 grams of the 10-octadecenoyl chloride adduct prepared in Example 18. The product, N,N- bis[9-(1,4,5,6,7,7-hexachlorobicyclo- [2.2.1]-5-heptene-2-yl)nonanoyl1piperazine, gave the following analysis: percent C, 44.90 (theory 44.84); percent H, 5.01 (theory 4.81); percent N, 2.73 (theory 2.91); percent Cl, 44.30 (theory 44.63).

The results of the screening evaluation of the products of Examples 1 to 20, compiled in Table 1, show their effectiveness as growth inhibitors against specific organisms.

We claim:

1. N-[8 (1,4,5,6,7,7-hexachloro-3-octylbicyclo[2.2.1]- 5 heptene-2-yl) oetanoyl] morpholine.

No references cited.

NICHOLAS S. RIZZO, Primary Examiner J. TOVAR, Assistant Examiner US. Cl. X.R. 

